Variant report

Variant	esv10021
Chromosome Location	chr1:243042294-243180836
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr1:243088083-243088303	K562	blood:	n/a	n/a
2	ATF1	chr1:243148543-243148578	K562	blood:	n/a	n/a
3	BACH1	chr1:243122482-243122506	K562	blood:	n/a	n/a
4	BATF	chr1:243178561-243178941	GM12878	blood:	n/a	n/a
5	BATF	chr1:243174180-243174389	GM12878	blood:	n/a	n/a
6	BATF	chr1:243178503-243178928	GM12878	blood:	n/a	n/a
7	BATF	chr1:243171378-243171664	GM12878	blood:	n/a	n/a
8	BCL11A	chr1:243174177-243174356	GM12878	blood:	n/a	n/a
9	BCL11A	chr1:243171382-243171573	GM12878	blood:	n/a	n/a
10	BCL11A	chr1:243178625-243178904	GM12878	blood:	n/a	chr1:243178799-243178808
11	BCL11A	chr1:243169760-243169972	GM12878	blood:	n/a	n/a
12	BCL11A	chr1:243172627-243172798	GM12878	blood:	n/a	n/a
13	BCL11A	chr1:243178550-243178986	GM12878	blood:	n/a	chr1:243178799-243178808
14	BCL11A	chr1:243153505-243153675	GM12878	blood:	n/a	n/a
15	BHLHE40	chr1:243087986-243088483	K562	blood:	n/a	n/a
16	CBX3	chr1:243100093-243100300	K562	blood:	n/a	n/a
17	CBX3	chr1:243087941-243088379	K562	blood:	n/a	n/a
18	CBX3	chr1:243130209-243130606	K562	blood:	n/a	n/a
19	CBX3	chr1:243053418-243053739	K562	blood:	n/a	n/a
20	CCNT2	chr1:243129321-243129526	K562	blood:	n/a	n/a
21	CCNT2	chr1:243087975-243088306	K562	blood:	n/a	n/a
22	CEBPB	chr1:243072449-243072662	HepG2	liver:	n/a	chr1:243072592-243072603
23	CEBPB	chr1:243072507-243072681	IMR90	lung:	n/a	chr1:243072592-243072603
24	CEBPB	chr1:243088005-243088218	K562	blood:	n/a	n/a
25	CEBPB	chr1:243118268-243118571	HepG2	liver:	n/a	chr1:243118438-243118447 chr1:243118436-243118449 chr1:243118438-243118447 chr1:243118438-243118447 chr1:243118436-243118449 chr1:243118436-243118447 chr1:243118437-243118448 chr1:243118438-243118447
26	CEBPB	chr1:243105243-243105313	A549	lung:	n/a	chr1:243105272-243105283
27	CEBPB	chr1:243118255-243118634	K562	blood:	n/a	chr1:243118438-243118447 chr1:243118436-243118449 chr1:243118438-243118447 chr1:243118438-243118447 chr1:243118436-243118449 chr1:243118436-243118447 chr1:243118437-243118448 chr1:243118438-243118447
28	CEBPB	chr1:243105260-243105310	HepG2	liver:	n/a	chr1:243105272-243105283
29	CEBPB	chr1:243118300-243118585	A549	lung:	n/a	chr1:243118438-243118447 chr1:243118436-243118449 chr1:243118438-243118447 chr1:243118438-243118447 chr1:243118436-243118449 chr1:243118436-243118447 chr1:243118437-243118448 chr1:243118438-243118447
30	CEBPB	chr1:243118303-243118616	K562	blood:	n/a	chr1:243118438-243118447 chr1:243118436-243118449 chr1:243118438-243118447 chr1:243118438-243118447 chr1:243118436-243118449 chr1:243118436-243118447 chr1:243118437-243118448 chr1:243118438-243118447
31	CEBPB	chr1:243118344-243118540	K562	blood:	n/a	chr1:243118438-243118447 chr1:243118436-243118449 chr1:243118438-243118447 chr1:243118438-243118447 chr1:243118436-243118449 chr1:243118436-243118447 chr1:243118437-243118448 chr1:243118438-243118447
32	CEBPB	chr1:243072543-243072743	K562	blood:	n/a	chr1:243072592-243072603
33	CEBPB	chr1:243118280-243118602	IMR90	lung:	n/a	chr1:243118438-243118447 chr1:243118436-243118449 chr1:243118438-243118447 chr1:243118438-243118447 chr1:243118436-243118449 chr1:243118436-243118447 chr1:243118437-243118448 chr1:243118438-243118447
34	CEBPB	chr1:243118288-243118578	Hela-S3	cervix:	n/a	chr1:243118438-243118447 chr1:243118436-243118449 chr1:243118438-243118447 chr1:243118438-243118447 chr1:243118436-243118449 chr1:243118436-243118447 chr1:243118437-243118448 chr1:243118438-243118447
35	CEBPB	chr1:243148513-243148717	K562	blood:	n/a	n/a
36	CHD2	chr1:243080927-243080928	K562	blood:	n/a	n/a
37	CHD2	chr1:243087993-243088116	K562	blood:	n/a	n/a
38	CTCF	chr1:243174278-243174346	K562	blood:	n/a	chr1:243174284-243174291
39	CTCF	chr1:243100200-243100350	GM12873	blood:	n/a	chr1:243100235-243100245 chr1:243100227-243100248 chr1:243100232-243100250 chr1:243100233-243100249 chr1:243100238-243100247
40	CTCF	chr1:243174203-243174412	GM12892	blood:	n/a	chr1:243174284-243174291
41	CTCF	chr1:243100146-243100354	GM19240	blood:	n/a	chr1:243100235-243100245 chr1:243100227-243100248 chr1:243100232-243100250 chr1:243100233-243100249 chr1:243100238-243100247
42	CTCF	chr1:243174248-243174356	GM10248	blood:	n/a	chr1:243174284-243174291
43	CTCF	chr1:243100220-243100370	GM06990	blood:	n/a	chr1:243100235-243100245 chr1:243100227-243100248 chr1:243100232-243100250 chr1:243100233-243100249 chr1:243100238-243100247
44	CTCF	chr1:243174100-243174250	MCF-7	breast:	n/a	n/a
45	CTCF	chr1:243049620-243049764	GM19238	blood:	n/a	n/a
46	CTCF	chr1:243100160-243100310	GM12869	blood:	n/a	chr1:243100235-243100245 chr1:243100227-243100248 chr1:243100232-243100250 chr1:243100233-243100249 chr1:243100238-243100247
47	CTCF	chr1:243174167-243174317	H1-hESC	embryonic stem cell:	n/a	chr1:243174284-243174291
48	CTCF	chr1:243148111-243148176	MCF-7	breast:	n/a	n/a
49	CTCF	chr1:243099997-243100378	A549	lung:	n/a	chr1:243100235-243100245 chr1:243100227-243100248 chr1:243100232-243100250 chr1:243100233-243100249 chr1:243100238-243100247
50	CTCF	chr1:243099989-243100475	A549	lung:	n/a	chr1:243100235-243100245 chr1:243100227-243100248 chr1:243100232-243100250 chr1:243100233-243100249 chr1:243100238-243100247

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:243139525-243139575	GM19239	blood:	n/a
2	chr1:243053865-243053915	HCPEpiC	choroid plexus:	n/a
3	chr1:243053425-243053475	HCPEpiC	choroid plexus:	n/a
4	chr1:243139525-243139575	GM19239	blood:	n/a
5	chr1:243053865-243053915	HCPEpiC	choroid plexus:	n/a
6	chr1:243053425-243053475	HCPEpiC	choroid plexus:	n/a
7	chr1:243054071-243054121	HL-60	blood:	n/a
8	chr1:243054071-243054121	BJ	skin:	n/a
9	chr1:243057080-243057130	A549	lung:	n/a
10	chr1:243138527-243138577	T-47D	breast:	n/a
11	chr1:243053865-243053915	HCM	heart:	n/a
12	chr1:243054071-243054121	ECC-1	luminal epithelium:	n/a
13	chr1:243053673-243053723	PANC-1	pancreas:	n/a
14	chr1:243053934-243053984	U87	brain:	n/a
15	chr1:243053425-243053475	SK-N-SH	brain:	n/a
16	chr1:243053425-243053475	BE2_C	brain:	n/a
17	chr1:243138527-243138577	HCPEpiC	choroid plexus:	n/a
18	chr1:243138527-243138577	HepG2	liver:	n/a
19	chr1:243138527-243138577	AG09319	gingival:	n/a
20	chr1:243053673-243053723	NH-A	brain:	n/a
21	chr1:243054071-243054121	HCPEpiC	choroid plexus:	n/a
22	chr1:243054071-243054121	PANC-1	pancreas:	n/a
23	chr1:243053934-243053984	PFSK-1	brain:	n/a
24	chr1:243053934-243053984	HAEpiC	amniotic membrane:	n/a
25	chr1:243050875-243050925	Hepatocyte	liver:	n/a
26	chr1:243050875-243050925	PrEC	prostate:	n/a
27	chr1:243053865-243053915	GM12878	blood:	n/a
28	chr1:243053934-243053984	Hepatocyte	liver:	n/a
29	chr1:243054071-243054121	ovcar-3	ovarian:	n/a
30	chr1:243053425-243053475	HNPCEpiC	eye:	n/a
31	chr1:243053934-243053984	LNCaP	prostate:	n/a
32	chr1:243054071-243054121	GM12878	blood:	n/a
33	chr1:243054071-243054121	NHBE	bronchial:	n/a
34	chr1:243139525-243139575	CMK	blood:	n/a
35	chr1:243053865-243053915	H1-hESC	embryonic stem cell:	embryo
36	chr1:243138527-243138577	HEEpiC	esophagus:	n/a
37	chr1:243053425-243053475	ECC-1	luminal epithelium:	n/a
38	chr1:243053673-243053723	NHDF-neo	bronchial:	n/a
39	chr1:243053865-243053915	IMR90	lung:	fetal
40	chr1:243053425-243053475	Jurkat	blood:	n/a
41	chr1:243138527-243138577	BJ	skin:	n/a
42	chr1:243138527-243138577	HCT-116	colon:	n/a
43	chr1:243054071-243054121	MCF10A-Er-Src	breast:	n/a
44	chr1:243057080-243057130	HRE	kidney:	n/a
45	chr1:243050875-243050925	PANC-1	pancreas:	n/a
46	chr1:243053425-243053475	A549	lung:	n/a
47	chr1:243138527-243138577	GM19239	blood:	n/a
48	chr1:243057080-243057130	HAEpiC	amniotic membrane:	n/a
49	chr1:243053865-243053915	Hepatocyte	liver:	n/a
50	chr1:243139525-243139575	HRPEpiC	eye:	n/a

No.	Distal block	Cell Line	Cell type
1	chr1:243080510..243082193-chr1:243083721..243085385,2	K562	blood:
2	chr1:243174257..243175773-chr22:20004723..20006804,2	K562	blood:
3	chr1:243080510..243082193-chr1:243083721..243085385,2	K562	blood:
4	chr1:242991254..242992220-chr1:243099841..243100636,3	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-CEP170-7	chr1:243078426-243078834	expReg_chr1_22680_-
2	lnc-CEP170-3	chr1:243169714-243169980	XLOC_001282
3	lnc-CEP170-9	chr1:243076529-243076866	refGeneNc_994_NR_026778
4	lnc-CEP170-3	chr1:243170676-243170770	XLOC_001282
5	lnc-CEP170-3	chr1:243169147-243169576	XLOC_001282
6	lnc-CEP170-8	chr1:243077153-243077520	expReg_chr1_22679_-
7	lnc-CEP170-9	chr1:243070564-243075269	refGeneNc_994_NR_026778
8	lnc-CEP170-9	chr1:243076807-243077141	expReg_chr1_22678_-

Variant related genes	Relation type
ENSG00000234116	TF binding region
ENSG00000230199	TF binding region
ENSG00000270818	TF binding region
ENSG00000264972	TF binding region
ENSG00000234116	CpG island
ENSG00000230199	CpG island
ENSG00000270818	CpG island
ENSG00000264972	CpG island
LEFTY2	miRNA target sites
LEPREL4	miRNA target sites

Extended variants
information (count: 1873 )
Associated
traits (count: 95 )

Variant overlapped rSNPs/rCNVs (count:1873 , 50 per page) page: 1 2 3 4 5 6 7 ... 38

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs577403554	chr1:243042303-243042304	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs541712411	chr1:243042358-243042359	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs372201507	chr1:243042361-243042362	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs67638427	chr1:243042362-243042363	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs538566337	chr1:243042363-243042364	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs398050190	chr1:243042378-243042379	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs76176281	chr1:243042379-243042380	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs80012548	chr1:243042380-243042381	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs73130195	chr1:243042397-243042398	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs113096003	chr1:243042420-243042421	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs373565425	chr1:243042471-243042472	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs543873773	chr1:243042515-243042516	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs147545677	chr1:243042587-243042588	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs140208543	chr1:243042599-243042600	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs529413913	chr1:243042607-243042608	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs369216968	chr1:243042650-243042651	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs549175574	chr1:243042712-243042713	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs114123699	chr1:243042785-243042786	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs145610970	chr1:243042790-243042791	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs547568054	chr1:243042796-243042797	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs182772490	chr1:243042817-243042818	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs113481044	chr1:243042858-243042859	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs114959487	chr1:243042876-243042877	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs4271198	chr1:243042891-243042892	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
25	rs188096500	chr1:243042894-243042895	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs191685785	chr1:243042924-243042925	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs7524043	chr1:243042933-243042934	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs565761966	chr1:243042936-243042937	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs184602817	chr1:243042959-243042960	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs575084400	chr1:243042960-243042961	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs558370142	chr1:243043006-243043007	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs578257613	chr1:243043035-243043036	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs542110011	chr1:243043055-243043056	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs188919811	chr1:243043064-243043065	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs557407804	chr1:243043076-243043077	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs7526395	chr1:243043086-243043087	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
37	rs543112080	chr1:243043101-243043102	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs77111625	chr1:243043125-243043126	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs75243876	chr1:243043165-243043166	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs554394373	chr1:243043166-243043167	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs6687165	chr1:243043167-243043168	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
42	rs540854583	chr1:243043168-243043169	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs529421213	chr1:243043215-243043216	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs12064942	chr1:243043247-243043248	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
45	rs563866483	chr1:243043284-243043285	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs533073443	chr1:243043290-243043291	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs549622129	chr1:243043294-243043295	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs6687294	chr1:243043342-243043343	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
49	rs6684664	chr1:243043346-243043347	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
50	rs548952967	chr1:243043348-243043349	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:95)

Disease	PMID	Source
Esophageal squamous carcinoma	21637470	CNVD
HIV/AIDS	22032296	CNVD
Schizophrenia	19415332	CNVD
Melanoma	18172304	CNVD
Rett syndrome	21593744	CNVD
Medulloblastoma	21979893	CNVD
Wilms tumour	21544195	CNVD
Breast cancer	17133270	CNVD
Non-small cell lung cancer	21044232	CNVD
Cervical cancer	21063398	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	20632083	CNVD
Endometrial cancer	22040021	CNVD
Ewing''s sarcoma	21437220	CNVD
Gastrointestinal stromal cancer	20470368	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	21080181	CNVD
Hepatocellular carcinoma	22174799	CNVD
Medulloblastoma	21292688	CNVD
Phyllodes tumor	17334353	CNVD
Breast cancer	21264507	CNVD
Liposarcoma	21253554	CNVD
Multiple myeloma	21628407	CNVD
Cancer	16751803	CNVD
Prostate cancer	16705090	CNVD
Neuroblastoma	19435921	CNVD
Breast cancer	17850661	CNVD
Breast cancer	16461572	CNVD
Intracranial tumor	16823260	CNVD
Medulloblastoma	18056178	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Colorectal cancer	16272173	CNVD
Neuroblastoma	21899760	CNVD
Breast cancer	21858162	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Breast cancer	16608533	CNVD
Ewing''s sarcoma	22429812	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Breast cancer	17001317	CNVD
Acute myeloid leukemia	21251322	CNVD
Multiple myeloma	17550852	CNVD
Acute myeloid leukemia	20729466	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Testicular germ cell tumor	18059402	CNVD
Ependymoma	18628472	CNVD
Leukemia	18628472	CNVD
Neuroblastoma	18923191	CNVD
Acute lymphoblastic leukemia	19100363	CNVD
Breast cancer	21509527	CNVD
Urothelial carcinoma	21177765	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Chordoma	18071362	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Hepatocellular carcinoma	18803288	CNVD
Urothelial tumor	18831757	CNVD
Lung cancer	18438408	CNVD
Medulloblastoma	16783165	CNVD
Basal cell lymphoma	17170743	CNVD
Basal cell lymphoma	17053054	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Congenital abnormalities	21549014	CNVD
Developmental delay	21549014	CNVD
Mental retardation	21549014	CNVD
small cell lung cancer	20016488	CNVD
Cancer	20164920	CNVD
Cancer	17060936	CNVD
abnormal development	18461090	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Non-small cell lung cancer	21829676	CNVD
Hepatocellular carcinoma	16750200	CNVD
Arrhythmogenic right ventricular cardiomyopathy	17576883	CNVD
Multiple myeloma	16616336	CNVD
Developmental delay	21147756	CNVD
Ovarian cancer	21720365	CNVD
Glioblastoma multiforme	22291905	CNVD
Myelofibrosis	22110671	CNVD
Disease	21936942	CNVD
laryngomalacia	21936942	CNVD
GLUT3 deficiency syndrome	20509907	CNVD
Developmental delay	21373258	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
Developmental delay	19490664	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Breast cancer	22522925	CNVD
Cancer	20164919	CNVD
Ovarian cancer	21781307	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:97 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:243041000-243043800	Weak transcription	Right Atrium	heart
2	chr1:243041000-243046600	Weak transcription	Pancreas	Pancrea
3	chr1:243042000-243042600	Enhancers	H9 Cell Line	embryonic stem cell
4	chr1:243042200-243044400	Weak transcription	Fetal Heart	heart
5	chr1:243044400-243045400	Enhancers	Fetal Heart	heart
6	chr1:243046600-243046800	Enhancers	Pancreas	Pancrea
7	chr1:243046800-243053600	Weak transcription	Pancreas	Pancrea
8	chr1:243047200-243049000	Weak transcription	A549	lung
9	chr1:243049000-243049200	Enhancers	A549	lung
10	chr1:243049200-243049800	Enhancers	ES-I3 Cell Line	embryonic stem cell
11	chr1:243049200-243049800	Enhancers	Liver	Liver
12	chr1:243049200-243049800	Enhancers	Rectal Mucosa Donor 31	rectum
13	chr1:243049200-243049800	Enhancers	Sigmoid Colon	Sigmoid Colon
14	chr1:243049200-243049800	Flanking Active TSS	A549	lung
15	chr1:243049200-243049800	Enhancers	HepG2	liver
16	chr1:243049600-243049800	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
17	chr1:243049800-243050600	Enhancers	A549	lung
18	chr1:243049800-243053600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
19	chr1:243049800-243053600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
20	chr1:243050600-243051800	Weak transcription	A549	lung
21	chr1:243053400-243053600	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
22	chr1:243053600-243053800	Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
23	chr1:243053600-243054000	Active TSS	ES-I3 Cell Line	embryonic stem cell
24	chr1:243053600-243054000	Active TSS	H1 Cell Line	embryonic stem cell
25	chr1:243053600-243054000	Flanking Active TSS	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
26	chr1:243053600-243054000	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
27	chr1:243053600-243054000	Bivalent/Poised TSS	H9 Derived Neuron Cultured Cells	ES cell derived
28	chr1:243053600-243054000	Active TSS	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
29	chr1:243053600-243054000	Active TSS	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
30	chr1:243053600-243054000	Active TSS	HUES6 Cell Line	embryonic stem cell
31	chr1:243053600-243054000	Active TSS	iPS-18 Cell Line	embryonic stem cell
32	chr1:243053600-243054000	Active TSS	iPS DF 6.9 Cell Line	embryonic stem cell
33	chr1:243053600-243054000	Flanking Active TSS	iPS DF 19.11 Cell Line	embryonic stem cell
34	chr1:243053600-243054000	Bivalent Enhancer	Breast Myoepithelial Primary Cells	Breast
35	chr1:243053600-243054000	Bivalent Enhancer	Foreskin Melanocyte Primary Cells skin01	Skin
36	chr1:243053600-243054000	Bivalent Enhancer	Foreskin Melanocyte Primary Cells skin03	Skin
37	chr1:243053600-243054000	Bivalent Enhancer	Brain Hippocampus Middle	brain
38	chr1:243053600-243054000	Enhancers	Fetal Brain Male	brain
39	chr1:243053600-243054000	Bivalent/Poised TSS	Fetal Brain Female	brain
40	chr1:243053600-243054000	Bivalent Enhancer	Fetal Muscle Trunk	muscle
41	chr1:243053600-243054000	Enhancers	Pancreas	Pancrea
42	chr1:243053600-243054000	Enhancers	Placenta Amnion	Placenta Amnion
43	chr1:243053600-243054000	Bivalent Enhancer	HMEC	breast
44	chr1:243053600-243054200	Active TSS	HUES48 Cell Line	embryonic stem cell
45	chr1:243053600-243054200	Active TSS	HUES64 Cell Line	embryonic stem cell
46	chr1:243053600-243054200	Active TSS	iPS-15b Cell Line	embryonic stem cell
47	chr1:243053600-243054200	Active TSS	iPS-20b Cell Line	embryonic stem cell
48	chr1:243053600-243054200	Active TSS	Brain Germinal Matrix	brain
49	chr1:243053600-243054200	Active TSS	HSMM	muscle
50	chr1:243053800-243054000	Flanking Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain

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